Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the RORC gene.

Also known as: IMD42, RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency, autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC, immunodeficiency 42, immunodeficiency type 42

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency itself.